Cas no 73931-66-5 (1-Naphthalenebutanoicacid, g-oxo-, ethyl ester)

1-Naphthalenebutanoic acid, γ-oxo-, ethyl ester is a specialized organic compound featuring a naphthalene core linked to a butanoic acid derivative with a γ-ketoester functional group. This structure imparts reactivity suitable for use as an intermediate in synthetic organic chemistry, particularly in the construction of complex molecules. The ethyl ester moiety enhances solubility in organic solvents, facilitating handling in various reaction conditions. Its γ-oxo group offers a versatile site for further functionalization, making it valuable in pharmaceutical and agrochemical synthesis. The compound’s well-defined structure ensures consistent performance in applications requiring precise molecular architecture. Proper storage under inert conditions is recommended to maintain stability.
1-Naphthalenebutanoicacid, g-oxo-, ethyl ester structure
73931-66-5 structure
Product Name:1-Naphthalenebutanoicacid, g-oxo-, ethyl ester
CAS No:73931-66-5
MF:C16H16O3
MW:256.296444892883
MDL:MFCD01320262
CID:576898
PubChem ID:233194
Update Time:2025-06-08

1-Naphthalenebutanoicacid, g-oxo-, ethyl ester Chemical and Physical Properties

Names and Identifiers

    • 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester
    • Ethyl 4-(1-naphthyl)-4-oxobutyrate
    • ethyl 4-naphthalen-1-yl-4-oxobutanoate
    • ethyl 4-(1-naphthyl)-4-oxobutanoate
    • ethyl 4-(naphthalen-1-yl)-4-oxobutanoate
    • ETHYL4-(1-NAPHTHYL)-4-OXOBUTYRATE
    • MFCD01320262
    • DTXSID60283418
    • NSC-31354
    • AKOS005944129
    • NSC31354
    • NSC 31354
    • 73931-66-5
    • MDL： MFCD01320262
    • Inchi： 1S/C16H16O3/c1-2-19-16(18)11-10-15(17)14-9-5-7-12-6-3-4-8-13(12)14/h3-9H,2,10-11H2,1H3
    • InChI Key： XWRHWEPJARAHBP-UHFFFAOYSA-N
    • SMILES： O(CC)C(CCC(C1C=CC=C2C=CC=CC=12)=O)=O

Computed Properties

  • Exact Mass: 256.11000
  • Monoisotopic Mass: 256.11
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 6
  • Complexity: 324
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3
  • Topological Polar Surface Area: 43.4?2

Experimental Properties

  • Density: 1.141
  • Boiling Point: 419.3°C at 760 mmHg
  • Flash Point: 186.6°C
  • Refractive Index: 1.577
  • PSA: 43.37000
  • LogP: 3.36580

1-Naphthalenebutanoicacid, g-oxo-, ethyl ester Customs Data

  • HS CODE：2918300090
  • Customs Data：

    China Customs Code:

    2918300090

    Overview:

    2918300090 Other aldehydes or ketones without other oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%

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1-Naphthalenebutanoicacid, g-oxo-, ethyl ester Suppliers

Amadis Chemical Company Limited
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Audited Supplier Audited Supplier
(CAS:73931-66-5)1-Naphthalenebutanoicacid, g-oxo-, ethyl ester
Order Number:A1173461
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 01:25
Price ($):287.0

1-Naphthalenebutanoicacid, g-oxo-, ethyl ester Related Literature

Additional information on 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester

Recent Advances in the Study of 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester (CAS: 73931-66-5)

The compound 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester (CAS: 73931-66-5) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug development and therapeutic interventions. This research briefing aims to provide an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential clinical applications.

Recent studies have highlighted the unique chemical properties of 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester, which make it a promising candidate for the development of novel therapeutic agents. Researchers have successfully synthesized this compound using advanced organic chemistry techniques, and its structural characterization has been confirmed through spectroscopic methods such as NMR and mass spectrometry. The compound's stability and reactivity under various conditions have also been investigated, providing valuable insights for its potential use in pharmaceutical formulations.

In terms of biological activity, preliminary in vitro studies have demonstrated that 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester exhibits significant inhibitory effects on certain enzymes involved in inflammatory pathways. These findings suggest its potential as an anti-inflammatory agent, with possible applications in the treatment of chronic inflammatory diseases. Additionally, the compound has shown moderate cytotoxicity against specific cancer cell lines, indicating its potential as a lead compound for anticancer drug development.

Further research has explored the pharmacokinetic properties of 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester, including its absorption, distribution, metabolism, and excretion (ADME) profiles. These studies have revealed that the compound has favorable bioavailability and metabolic stability, which are crucial factors for its development as a therapeutic agent. However, more extensive in vivo studies are needed to fully understand its safety and efficacy profiles.

In conclusion, 1-Naphthalenebutanoicacid, g-oxo-, ethyl ester (CAS: 73931-66-5) represents a promising compound with potential applications in drug discovery and development. Its unique chemical properties, combined with its demonstrated biological activity, make it a valuable subject for further research. Future studies should focus on optimizing its synthesis, elucidating its mechanism of action, and evaluating its therapeutic potential in preclinical and clinical settings.

73931-66-5 (1-Naphthalenebutanoicacid, g-oxo-, ethyl ester) Related Products

Recommended suppliers
Amadis Chemical Company Limited
(CAS:73931-66-5)1-Naphthalenebutanoicacid, g-oxo-, ethyl ester
A1173461
Purity:99%
Quantity:1g
Price ($):287.0
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